Low frequency and Microwave Magnetoelectric Effects in Thick Film Heterostructures of Lithium Zinc Ferrite and Lead Zirconate Titanate

Magnetoelectric (ME) coupling at low frequencies and at x-band have been investigated in layered samples containing zinc substituted lithium ferrite and lead zirconate titanate (PZT). Multilayers of Li0.5-x/2ZnxFe2.5-x/2O4 (LZFO) (x=0-0.4) and PZT were prepared by lamination and sintering of thick films. At low frequencies (10-1000 Hz), the ME voltage coefficient for transverse fields is higher than for longitudinal fields. With Zn substitution in the ferrite, transverse coupling increases to a maximum for x=0.3 and then decreases for higher x. Analysis based on our model for a bilayer implies an efficient magneto-mechanical coupling with Zn substitution, resulting in strong ME interactions. Microwave ME coupling is studied through measurements of shift in the ferromagnetic resonance field due to an applied electric field. Estimated ME constants from such data are in agreement with our model for a ferrite-PZT bilayer.Comment: To be published in Solid State Communication

Linearized cloudpoint curve correlation for ternary systems consisting of one polymer, one solvent and one non-solvent

A linear correlation function is found for cloudpoint composition curves of ternary systems consisting of one polymer, one solvent and one non-solvent. The conditions for validity of this correlation function appear to be that the polymer is strongly incompatible with the non-solvent, and that only liquid-liquid demixing occurs. The linearized cloudpoint (LCP) curve is interpreted in terms of the various parameters occurring in the Flory-Huggins theory. The slope of the LCP line appears to be only dependent on the molar volumes of the components. Information about the binary Flory-Huggins interaction parameters and their concentration dependence can be obtained from the intercept of the linearized curve. Cloudpoints induced by crystallization do not follow the correlation. This gives an opportunity to distinguish between crystallization and liquid-liquid demixing without any additional experiments

Mass transfer and thermodynamics during immersion precipitation for a two-polymer system: Evaluation with the system PES-PVP-NMP-water

An extended version of the mass transfer model by Reuvers et al. for a four-component system is evaluated, which is shown to be generally valid for short times. The thermodynamics under these circumstances are evaluated, together with the kinetics. Initial composition paths (concentration profiles) are calculated. It appears that delay of demixing is not possible when a polymeric additive is used, which is soluble in the nonsolvent, while the velocity of demixing decreases. The calculations are evaluated for the system poly(ether sulfone)-poly(vinylpyrrolidone)-N-methylpyrrolidone-water by means of light transmission measurements during immersion precipitation, for a wide range of compositions of the polymer solution and coagulation bath

Tailoring of ferromagnetic Pr0.85Ca0.15MnO3/ferroelectric Ba0.6Sr0.4TiO3 superlattices for multiferroic properties

Superlattices composed of ferromagnetic Pr0.85Ca0.15MnO3 and ferroelectric Ba0.6Sr0.4TiO3 layers were fabricated on (100) SrTiO3 substrates by a pulsed-laser deposition method. The capacitance and resistive parts of the samples were analyzed from the complex impedance measurements, performed on the samples using a special experimental set-up. The superlattice with larger ferroelectric thickness shows unique characteristics which are not present in the parent ferromagnetic thin film. The superlattice show both ferromagnetic and ferroelectric transitions which is an evidence for the coexistence of both the properties. The high magnetoresistance (40 % at 80K) shown by the superlattice can be attributed to the coupling between ferromagnetic and ferroelectric layers, i.e, to the magnetoelectric effect.Comment: To be published in App. Phys. Let

Microstructures in phase inversion membranes. Part II. The role of a polymeric additive

Membranes were prepared from a casting solution of a water-soluble polymer, poly (vinyl pyrrolidone) (PVP), and a membrane forming polymer, poly (ether sulfone), in 1-methyl-2-pyrrolidone (NMP) as solvent by immersing them in mixtures of water and NMP. It was found that the addition of PVP to the ternary system suppresses the formation of macrovoids in the sub-layer, while the ultrafiltration-type top-layer consists of a closely packed layer of nodules. Using a model for pass transfer in this quaternary system, it is possible to explain the effects of the additive on macrovoid formation. Strong indications are found that the appearance of a nodular structure in the top-layer follows a mechanism of spinodal decomposition during the very early stages of the immersion step

A new spinning technique for hollow fiber ultrafiltration membranes

A new spinning technique for hollow fiber membranes with a densified outer toplayer has been developed in our laboratory. This technique makes use of a new type of spinneret having three concentric orifices. Apart from polymer solution and bore liquid as applied in classical spinnerets a third liquid can be pumped through an outer layer. After a certain contact time with the third liquid the nascent hollow fiber membrane meets the coagulation bath. This spinning technique has been applied to produce hollow fiber ultrafiltration membranes. The presence of poly-vinylpyrrolidone in the polymer solution is shown to be essential to induce a porous toplayer. Membranes having a waterflux of 275 L-m-2-hr-1-bar-1 and BSA retention of 97% have been spun. Although more research has to be done the first results seem to be very promising

Spinning of hollow fiber ultrafiltration membranes from a polymer blend

In this study the dry-wet spinning technique is used for the preparation of hollow fiber membranes. In the polymer solution a blend of two polymers, poly(ether sulfone) and poly(vinyl pyrrolidone), is used. The morphology of the membranes obtained is related to rheological characteristics and phase behavior of the polymer solution during spinning. The outer surface pore structure is mainly dependent on the conditions in the airgap. The typical performance of the membranes lies in the ultrafiltration region

Dilation kinetics of glassy, aromatic polyimides induced by carbon dioxide sorption

Over the past years, the equilibrium sorption of gases in polymers has been intensively studied. Mostly, glassy polymers were investigated because of their excellent selective mass transport properties. This work does not focus on the equilibrium sorption but on the kinetics to reach the equilibrium. We developed a new experimental method measuring the sorption-induced dilation kinetics of a polymer film. Carbon dioxide and glassy, aromatic polyimides were chosen as model systems. Low-pressure experiments demonstrate that the measured dilation kinetics represent the sorption kinetics. A significant delay between the sorption and dilation kinetics is based on the fact that dilation kinetics occurs simultaneously with the concentration increase in the center of the polymer film. High-pressure experiments reveal significant differences in dilation kinetics compared to low-pressure experiments. Generally, three regimes can be distinguished in the dilation kinetics: a first, fast volume increase followed by two much slower regimes of volume increase. The magnitude of fast and slow dilation kinetics strongly depends on the swelling history of the polymer sample. The results of the experiments are analyzed in the light of a model relating the fast dilation kinetics to a reversible Fickian dilation and the slower dilation kinetics to an irreversible, relaxational dilation